Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Chloroacetaldehyde → N-(pyridin-2-yl)thiazol-2-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Chloroacetaldehyde | HCID 33 | — |
| 반응물 | Urea | HCID 1176 | — |
| 반응물 | 1-(2-Pyridyl)-2-thiourea | HCID 1490491 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | N-(pyridin-2-yl)thiazol-2-amine | HCID 956683 | — |
반응 단계
To a flask was added 2-pyridyl thiourea (5-1) (3.48 g, 22.7 mmol), 3 mL ethanol, and 50% by weight chloroacetaldehyde (14.4 mL, 113.5 mol). The flask was then heated to reflux. As the mixture was heated, the urea slowly dissolved in solution. After 3 hours, the ethanol was removed under reduced pressure. Saturated aqueous NaHCO3 was then added to the flask and a white precipitate formed after vigorous bubbling. The precipitate was filtered and washed with water. The white solid was then dried under vacuum overnight with P2O5 drying agent. 1H NMR (CDCl3): δ 10.95 (bs, 1H), 8.37 (d, 1H, J=4.2 Hz), 7.61 (t, 1H, J=7.0 Hz), 7.49 (d, 1H, J=3.5 Hz), 6.94 (d, 1H, J=8.3 Hz), 6.88 (t, 1H, J=7.1 Hz), 6.85 (d, 1H, J=3.7 Hz).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06586424B2 |
| 출처 데이터셋 | uspto-grants-2003_07 |
| ORD ID | ord-4ace70b19ad34e819b949b436e2ab0a4 |
| 출처 메모 | uspto-grants-2003_07 |